gudid Primary ID: Ceramill Splintec 98x14 N/US

Ceramill Splintec (UDI Ceramill Splintec 98x14 N/US)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Ceramill Splintec (Model/Catalog Number: Ceramill Splintec 98x14 N/US) is a medical device manufactured by Merz Dental GmbH. This product is indexed under FDA Product Code / Category Classification MQC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Ceramill Splintec 98x14 N/US
Product Code / EMDN: MQC
Device Name: Ceramill Splintec 98x14 N/US
Database Sync Date: 2026-08-09 09:02:54

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Ceramill Splintec?

The registered manufacturer of record for Ceramill Splintec is Merz Dental GmbH.

What is the Primary UDI-DI identifier for Ceramill Splintec?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Ceramill Splintec 98x14 N/US.

What classification code is assigned to this device?

This device is registered under product classification code MQC.

Similar Classification Devices (MQC)

Other Devices by Merz Dental GmbH

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint